ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 881 • 2014 ACR/ARHP Annual Meeting

    DNA Methylation Analysis of the Temporal Artery Microenvironment Reveals a Robust T Cell Signature and Suggests a Role for TNF-α in Giant Cell Arteritis

    Patrick S. Coit1, Lindsey B. De Lott2, Bin Nan3, Victor M. Elner4 and Amr H. Sawalha1, 1Division of Rheumatology, University of Michigan, Ann Arbor, MI, 2Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, 3Department of Biostatistics, University of Michigan, Ann Arbor, MI, 4Department of Ophthalmology and Visual Sciences & Department of Pathology, University of Michigan, Ann Arbor, MI

    Background/Purpose: Giant cell arteritis (GCA) is a systemic large vessel vasculitis of unknown etiology. A hallmark of GCA is the presence of granulomatous inflammation of…
  • Abstract Number: 880 • 2014 ACR/ARHP Annual Meeting

    An Immunochip Study Confirms a Strong Contribution of HLA Class I and II Genes in the Susceptibility to Giant Cell Arteritis

    Francisco David Carmona1, Sarah Mackie2, Jose Ezequiel Martin1, John Taylor2, Augusto Vaglio3, Lara Bossini-Castillo1, Santos Castañeda4, Maria C. Cid5, José Hernández-Rodríguez6, Roser Solans7, Ricardo Blanco8, Lorenzo Beretta9, Claudio Lunardi10, Marco A. Cimmino11, Cisca Wijmenga12, Torsten Witte13, Julia Holle14, Frank Moosig14, Verena Schönau15, Andre Franke16, Øyvind Palm17, Andreas P. Diamantopoulos18, Benedicte A. Lie19, Simon Carette20, David Cuthbertson21, Gary S. Hoffman22, Nader A. Khalidi23, Curry L. Koening24, Carol A. Langford25, Carol McAlear26, Larry Moreland27, Paul A. Monach28, Christian Pagnoux20, Philip Seo29, Antoine G. Sreih30, Kenneth J. Warrington31, Steven R. Ytterberg31, Colin T. Pease32, Andrew Gough33, Michael Green34, Lesley Hordon35, Stephen Jarrett36, Richard Watts37, Sarah Levy38, Yusuf Patel39, Sanjeet Kamath40, Bhaskar Dasgupta41, Paul IW. de Bakker42, Bobby P.C. Koeleman42, Jennifer H. Barrett2, Carlo Salvarani43, Peter A. Merkel44, Miguel A. Gonzalez-Gay8, Ann W. Morgan2 and Javier Martin1, 1Immunology, Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Armilla (Granada), Spain, 2NIHR-Leeds Musculoskeletal Biomedical Research Unit, University of Leeds, Leeds, United Kingdom, 3Unit of Nephrology, University Hospital of Parma, Parma, Italy, 4Rheumatology, Hospital Universitario de La Princesa, IISP, Madrid, Spain, 5Vasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic University of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 08036- Barcelona, Spain, 6Vasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic University of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain, 7Autoimmune Systemic Diseases Unit, Department of Internal Medicine, Hospital Vall d'Hebron, Autonomous University of Barcelona, Barcelona, Spain, 8Department of Rheumatology, Hospital Universitario Marqués de Valdecilla, IFIMAV, Santander, Spain, 9Referral Center for Systemic Autoimmune Diseases, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico di Milano, Milan, Italy, 10Department of Medicine, Università degli Studi di Verona, Verona, Italy, 11Department of Internal Medicine, Academic Unit of Clinical Rheumatology, University of Genova, Genova, Italy, 12Department of Genetics, University Medical Hospital Groningen, University of Groningen, Groningen, Netherlands, 13Clinic for Immunology and Rheumatology, Hannover Medical School, Hannover, Germany, 14Vasculitis Clinic, Klinikum Bad Bramstedt & University Hospital of Schleswig Holstein, Bad Bramstedt, Germany, 15Department of Rheumatology and Immunology, Universitätsklinikum Erlangen, Erlangen, Germany, 16Institute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel, Kiel, Germany, 17Department of Rheumatology, Oslo University Hospital and University of Oslo, Oslo, Norway, 18Department of Rheumatology, Hospital of Southern Norway Trust, Kristiansand, Norway, 19Department of Medical Genetics, University of Oslo and Oslo University Hospital, Oslo, Norway, 20Division of Rheumatology, University of Toronto, Toronto, ON, Canada, 21Department of Biostatistics, University of South Florida, Tampa, FL, 22Center for Vasculitis Care and Research, Cleveland Clinic Foundation, Cleveland, OH, 23Division of Rheumatology, St. Joseph’s Hospital, McMaster University, Hamilton, ON, Canada, 24Division of Rheumatology, University of Utah, Salt Lake City, UT, 25Center for Vasculitis Care and Research, Cleveland Clinic, Cleveland, OH, 26Division of Rheumatology, Vasculitis Center, University of Pennsylvania, Philadelphia, PA, 27Rheumatology & Clinical Immunology, Vasculitis Center, of University of Pittsburgh Medical Center, Pittsburgh, PA, 28Section of Rheumatology, Vasculitis Center, Boston University School of Medicine, Boston, MA, 29Rheumatology Division, Johns Hopkins Vasculitis Center, Johns Hopkins University, Baltimore, MD, 30Medicine/Division of Rheumatology, The University of Pennsylvania, Philadelphia, PA, 31Division of Rheumatology, Mayo Clinic, Rochester, MN, 32Department of Rheumatology, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom, 33Department of Rheumatology, Harrogate and District Foundation Trust, Harrogate, United Kingdom, 34Department of Rheumatology, York Teaching Hospital NHS Foundation Trust, York, United Kingdom, 35Department of Rheumatology, Mid Yorkshire Hospitals NHS Trust, Dewsbury, United Kingdom, 36Department of Rheumatology, Mid Yorkshire Hospitals NHS Trust, Wakefield, United Kingdom, 37Department of Rheumatology, Ipswich Hospital NHS Trust, Ipswich, United Kingdom, 38Department of Rheumatology, Croydon Health Service NHS Trust, Croydon, United Kingdom, 39Department of Rheumatology, Hull and East Yorkshire NHS Trust, Hull East Yorkshire, United Kingdom, 40Department of Rheumatology, Staffordshire and Stoke-on-Trent Partnership NHS Trust, Staffordshire, United Kingdom, 41Department of Rheumatology, Southend University Hospital, Essex, United Kingdom, 42Department of Medical Genetics, University Medical Center Utrecht, Utrecht, Netherlands, 43Rheumatology Unit, Department of Internal Medicine, Azienda Ospedaliera ASMN, Istituto di Ricovero e Cura a Carattere Scientifico, Reggio Emilia, Italy, 44University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Giant cell arteritis (GCA) is a chronic autoimmune vasculitis with an important genetic component. We aimed to identify relevant risk loci for GCA predisposition…
  • Abstract Number: 899 • 2014 ACR/ARHP Annual Meeting

    Insurance Status and U.S. Region Associated with Placement of Permanent Vascular Access in Dialysis Patients with End-Stage Renal Disease Secondary to Lupus Nephritis

    Laura Plantinga1, Cristina M. Drenkard2, Rachel Patzer3, William McClellan1, Stephen Pastan4 and S. Sam Lim5, 1Department of Epidemiology, Emory University, Atlanta, GA, 2Medicine, Div Rheumatology, Emory University, Atlanta, GA, 3Department of Surgery, Emory University, Atlanta, GA, 4Department of Medicine, Division of Renal Medicine, Emory University, Atlanta, GA, 5Emory University School of Medicine, Division of Rheumatology, Atlanta, GA

    Background/Purpose: Prior data suggest sociodemographic and regional variability in various indicators of quality of end-stage renal disease (ESRD) care, both overall and in the SLE…
  • Abstract Number: 898 • 2014 ACR/ARHP Annual Meeting

    Traditional Cardiovascular Risk-Factor Management in Patients with Rheumatoid Arthritis Compared with Matched Non-Rheumatoid Arthritis Patients in a US Managed Care Setting

    J An1, K Reynolds2, E Alemao3, H Kawabata3, D H Solomon4, K P Liao5 and T C Cheetham2, 1Western University of Health Sciences, Pomona, CA, 2Kaiser Permanente Southern California, Pasadena, CA, 3Bristol-Myers Squibb, Princeton, NJ, 4Brigham and Women's Hospital, Boston, MA, 5Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA

    Background/Purpose: Studies have suggested suboptimal care of traditional cardiovascular risk factors (CRF) in patients (pts) with RA as a reason for elevated CV risk compared…
  • Abstract Number: 882 • 2014 ACR/ARHP Annual Meeting

    A Signature of microRNAs Overexpressed in Inflamed Temporal Arteries of Patients with Giant Cell Arteritis

    Stefania Croci1, Alessandro Zerbini1, Luigi Boiardi2, Francesco Muratore2, Alessandra Bisagni3, Giulia Pazzola2, Luca Cimino4, Antonio Moramarco4, Davide Nicoli5, Enrico Farnetti6, Bruno Casali6, Alberto Cavazza3, Maria Parmeggiani7 and Carlo Salvarani2, 1Clinical Immunology, Allergology and Advanced Biotechnologies Unit,, Arcispedale S Maria Nuova, Reggio Emilia, Italy, 2Rheumatology Unit, Arcispedale S Maria Nuova, Reggio Emilia, Italy, 3Pathology Unit, Arcispedale S Maria Nuova, Reggio Emilia, Italy, 4Ophthalmology Unit, Arcispedale S Maria Nuova, Reggio Emilia, Italy, 5Laboratory of Molecular Biology, Arcispedale S Maria Nuova, Reggio Emilia, Italy, 6Laboratory of Molecular Biology,, Arcispedale S Maria Nuova, Reggio Emilia, Italy, 7Clinical Immunology, Allergology and Advanced Biotechnologies Unit, Arcispedale S Maria Nuova, Reggio Emilia, Italy

    Background/Purpose: MicroRNAs (miRNAs) are small, non-coding RNAs that suppress gene expression at post-transcriptional level. MiRNAs can regulate innate and adaptive immunity. Moreover, they have been…
  • Abstract Number: 878 • 2014 ACR/ARHP Annual Meeting

    Luminex and Autoantigen Microarray Analysis of Sera from Patients with Diffuse Cutaneous Systemic Sclerosis Reveals Changes Associated with Imatinib Mesylate Treatment

    D. James Haddon1, Hannah Wand2, Paul J. Utz1, Robert F. Spiera3, Jessica K. Gordon3 and Lorinda Chung4, 1Medicine, Stanford University School of Medicine, Stanford, CA, 2Stanford University School of Medicine, Stanford, CA, 3Rheumatology, Hospital for Special Surgery, New York, NY, 4Immunology and Rheumatology, Stanford University School of Medicine, Palo Alto, CA

    Background/Purpose Tyrosine kinase inhibitors (TKIs), including imatinib mesylate, have been studied for the treatment of diffuse cutaneous Systemic Sclerosis (dcSSc). In a previously reported single…
  • Abstract Number: 877 • 2014 ACR/ARHP Annual Meeting

    Sildenafil Attenuates the Fibrotic Phenotype in Scleroderma Skin Fibroblasts

    Tomoaki Higuchi1, Yasushi Kawaguchi1, Kae Takagi1, Akiko Tochimoto1, Yuko Ota2, Yasuhiro Katsumata1, Takahisa Gono1, Masanori Hanaoka1, Yuko Okamoto1, Hidenaga Kawasumi1 and Hisashi Yamanaka3, 1Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 210-22 Kawada-Cha Shinjuku-Ku, Tokyo Women's Medical University, Tokyo, Japan, 3Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan

    Background/Purpose Systemic sclerosis (SSc) is a connective tissue disease characterized by inflammation, vasculopathy and fibrosis. Tissue fibrosis directly contributes to mortality or quality of life.…
  • Abstract Number: 876 • 2014 ACR/ARHP Annual Meeting

    SAR100842, an Antagonist of Lysophaphatidic Acid Receptor 1, As a Potential Treatment for Patients with Systemic Sclerosis: Results from a Phase 2a Study

    Dinesh Khanna1, Christopher P. Denton2, Alexandre Jagerschmidt3, Martine Jasson4, Oliver Distler5 and Yannick Allanore6, 1University of Michigan Scleroderma Program, Ann Arbor, MI, 2Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School Royal Free Campus, London, United Kingdom, 3Tissue Protection and Repear Unit, Sanofi-Aventis, Chilly-Mazarin, France, 4Clinical Development, Sanofi-Aventis, Paris, France, 5Center of Experimental Rheumatology, Zurich University Hospital, Zurich, Switzerland, 6Department of Rheumatology, University Paris Descartes and Cochin Hospital, Paris, France

    Background/Purpose Preclinical genetic and pharmacological studies suggest a role for Lysophosphatidic acid (LPA) involvement in three key processes of systemic sclerosis: fibrosis, microangiopathy and immunoinflammation.…
  • Abstract Number: 875 • 2014 ACR/ARHP Annual Meeting

    Treatment-Related Outcomes in Connective Tissue Disease-Associated Pulmonary Arterial Hypertension: A Pooled Analysis of 12 Randomized Controlled Trials

    Rennie L. Rhee1, Nicole B. Gabler2, Amy Praestgaard2, Peter A. Merkel3 and Steven M. Kawut4, 1Rheumatology, University of Pennsylvania, Philadelphia, PA, 2Department of Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia, PA, 3University of Pennsylvania, Philadelphia, PA, 4Pulmonary and Critical Care, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Recent studies have shown that therapies for pulmonary arterial hypertension (PAH) improve exercise capacity, but subgroup analyses suggest that these therapies may be less…
  • Abstract Number: 874 • 2014 ACR/ARHP Annual Meeting

    Safety and Efficacy of Subcutaneous Tocilizumab in Adults with Systemic Sclerosis: Week 24 Data from a Phase 2/3 Trial

    Dinesh Khanna1, Christopher P. Denton2, Jacob M. van Laar3, Angelika Jahreis4, Sabrina Cheng4, Helen Spotswood5, Jeffrey Siegel4 and Daniel E. Furst on behalf of FaSScinate Clinical Trial in Patients With SS6, 1University of Michigan Health System, Ann Arbor, MI, 2University College London Medical School, London, United Kingdom, 3University Medical Center Utrecht, Utrecht, Netherlands, 4Genentech, South San Francisco, CA, 5Roche Products Ltd., Welwyn Garden City, United Kingdom, 6University of California, Los Angeles, CA

    Background/Purpose: Systemic sclerosis (SSc) is a progressive, debilitating disease with limited treatment options. IL-6 has been implicated in disease pathogenesis.1,2 IL-6 receptor inhibition prevented and…
  • Abstract Number: 873 • 2014 ACR/ARHP Annual Meeting

    The Second Messenger, Cyclic GMP-AMP Dinucleotide (cGAMP) and the Enzyme, Cyclic GMP-AMP Synthase (cGAS), Are Expressed in Systemic Lupus Erythematosus

    Jie An1, Joshua Woodward2, Reynold Karr3, Thomas H. Teal4 and Keith B. Elkon1, 1Division of Rheumatology, University of Washington, Seattle, WA, 2Department of Microbiology, University of Washington, Seattle, WA, 3Department of Medicine, University of Washington, Seattle, WA, 4Rheumatology, University of Washington, Seattle, WA

    Background/Purpose: The type I IFNs (IFN-I), are strongly associated with Systemic Lupus Erythematosus (SLE).  It is generally considered that IFN-I is induced by immune complexes…
  • Abstract Number: 872 • 2014 ACR/ARHP Annual Meeting

    Interferon-α and Angiogenic Dysregulation in Pregnant Lupus Patients Destined for Preeclampsia

    Danieli Andrade1, Mimi Kim2, Luz P. Blanco3, S. Ananth Karumanchi4, Gloria Koo5, Patricia M. Redecha6, Kyriakos A. Kirou1, Angela M. Alvarez7, Melissa J. Mulla7, Mary K. Crow8, Vikki Abrahams7, Mariana J. Kaplan3 and Jane E. Salmon9, 1Hospital for Special Surgery, New York, NY, 2Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY, 3Systemic Autoimmunity Branch, Intramural Research Program, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 4Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 5Autoimmunity & Inflammation, Hospital for Special Surgery, New York, NY, 6Rheumatology Research, Hospital for Special Surgery, New York, NY, 7Yale School of Medicine, New Haven, CT, 8Department of Medicine, Hospital for Special Surgery, New York, NY, 9Rheumatology, Hospital for Special Surgery, New York, NY

    Background/Purpose: Pregnant patients with SLE are at increased risk of placental insufficiency and preeclampsia, disorders associated with angiogenic factor imbalance. IFN-α, a critical element in…
  • Abstract Number: 871 • 2014 ACR/ARHP Annual Meeting

    Antimalarials Regulate TLR7/8 Mediated Macrophage Activation Via Epigenetic Modification at the TNFα Promoter

    Androo J. Markham1,2, Mark Halushka3, Cristiana Guiducci4, Robert M. Clancy5 and Jill P. Buyon5, 1Medicine, New York University School of Medicine, New York, NY, 2Medicine, Equal contributing author, New York, NY, 3Division of Cardiovascular Pathology, John Hopkins Pathology, Baltimore, MD, 4Discovery Department, Dynavax Technologies, Berkeley, CA, 5Department of Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY

    Background/Purpose: Maternal anti-SSA autoantibodies contribute to the pathogenesis of congenital heart block by the formation of immune complexes (IC) comprised of Ro and ssRNA (hY3)…
  • Abstract Number: 870 • 2014 ACR/ARHP Annual Meeting

    IRF1 Influences on Histone H4 Acetylation in Systemic Lupus Erythematosus

    Yiu Tak Leung1, Lihua Shi2, Kelly Maurer2, Li Song2, Zhe Zhang3, Michelle Petri4 and Kathleen E. Sullivan2, 1Medicine/Rheumatology, University of Pennsylvania, Philadelphia, PA, 2Immunology ARC 1216, The Children's Hospital of Philadelphia, Philadelphia, PA, 3Bioinformatics, Bioinformatics, Children's Hospital of Philadelphia, Philadelphia, PA, 4Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Systemic lupus erythematosus (SLE) is the classical systemic autoimmune disease. Epigenetic processes, such as posttranslational histone modifications, can regulate gene expression without altering the…
  • Abstract Number: 869 • 2014 ACR/ARHP Annual Meeting

    UBE2L3 genotype Influences Plasma Cell Proliferation in Systemic Lupus Erythematosus By Regulation of NF-κB By the Linear Ubiquitination Assembly Complex

    Myles J. Lewis1, Simon Vyse1, Adrian M. Shields2, Sebastian Boeltz2, Patrick Gordon3, Timothy D. Spector4, Paul J. Lehner5, Henning Walczak6 and Timothy J. Vyse2, 1Experimental Medicine & Rheumatology, Queen Mary University of London, London, United Kingdom, 2Medical & Molecular Genetics, King's College London, London, United Kingdom, 3Department of Rheumatology, King's College London, London, United Kingdom, 4Department of Twin Research, King's College London, London, United Kingdom, 5Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom, 6Centre for Cell Death, Cancer and Inflammation, University College London, London, United Kingdom

    Background/Purpose: Genome-wide association studies have identified a strong association between a single risk haplotype of the UBE2L3gene and Systemic Lupus Erythematosus (SLE), as well as…
  • « Previous Page
  • 1
  • …
  • 2171
  • 2172
  • 2173
  • 2174
  • 2175
  • …
  • 2605
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

Embargo Policy

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology